Cancer Program, Biomedicine Discovery Institute, Monash University, Clayton, Australia.
Department of Biochemistry and Molecular Biology, Monash University, Clayton, Australia.
Mol Oncol. 2024 Jun;18(6):1437-1459. doi: 10.1002/1878-0261.13654. Epub 2024 Apr 16.
Different molecular classifications for gastric cancer (GC) have been proposed based on multi-omics platforms with the long-term goal of improved precision treatment. However, the GC (phospho)proteome remains incompletely characterized, particularly at the level of tyrosine phosphorylation. In addition, previous multiomics-based stratification of patient cohorts has lacked identification of corresponding cell line models and comprehensive validation of broad or subgroup-selective therapeutic targets. To address these knowledge gaps, we applied a reverse approach, undertaking the most comprehensive (phospho)proteomic analysis of GC cell lines to date and cross-validating this using publicly available data. Mass spectrometry (MS)-based (phospho)proteomic and tyrosine phosphorylation datasets were subjected to individual or integrated clustering to identify subgroups that were subsequently characterized in terms of enriched molecular processes and pathways. Significant congruence was detected between cell line proteomic and specific patient-derived transcriptomic subclassifications. Many protein kinases exhibiting 'outlier' expression or phosphorylation in the cell line dataset exhibited genomic aberrations in patient samples and association with poor prognosis, with casein kinase I isoform delta/epsilon (CSNK1D/E) being experimentally validated as potential therapeutic targets. Src family kinases were predicted to be commonly hyperactivated in GC cell lines, consistent with broad sensitivity to the next-generation Src inhibitor eCF506. In addition, phosphoproteomic and integrative clustering segregated the cell lines into two subtypes, with epithelial-mesenchyme transition (EMT) and proliferation-associated processes enriched in one, designated the EMT subtype, and metabolic pathways, cell-cell junctions, and the immune response dominating the features of the other, designated the metabolism subtype. Application of kinase activity prediction algorithms and interrogation of gene dependency and drug sensitivity databases predicted that the mechanistic target of rapamycin kinase (mTOR) and dual specificity mitogen-activated protein kinase kinase 2 (MAP2K2) represented potential therapeutic targets for the EMT and metabolism subtypes, respectively, and this was confirmed using selective inhibitors. Overall, our study provides novel, in-depth insights into GC proteomics, kinomics, and molecular taxonomy and reveals potential therapeutic targets that could provide the basis for precision treatments.
不同的胃癌分子分类已经基于多组学平台提出,其长期目标是提高精准治疗。然而,胃癌(磷酸化)蛋白质组仍然没有完全被描述,尤其是在酪氨酸磷酸化水平。此外,以前基于多组学的患者队列分层缺乏对相应细胞系模型的鉴定和对广泛或亚组选择性治疗靶点的综合验证。为了解决这些知识空白,我们采用了一种反向方法,对胃癌细胞系进行了迄今为止最全面的(磷酸化)蛋白质组学分析,并使用公开可用的数据对其进行了交叉验证。基于质谱(MS)的(磷酸化)蛋白质组学和酪氨酸磷酸化数据集被单独或集成聚类,以鉴定随后在丰富的分子过程和途径方面具有特征的亚组。在细胞系蛋白质组学和特定的患者衍生转录子分类之间检测到显著的一致性。在细胞系数据集表现出“异常”表达或磷酸化的许多蛋白激酶在患者样本中表现出基因组异常,并与预后不良相关,实验验证酪蛋白激酶 I 同工型 delta/epsilon(CSNK1D/E)作为潜在的治疗靶点。预测原癌基因Src 家族激酶在 GC 细胞系中经常过度激活,与新一代 Src 抑制剂 eCF506 的广泛敏感性一致。此外,磷酸化蛋白质组学和整合聚类将细胞系分为两个亚类,上皮-间充质转化(EMT)和增殖相关过程在一个亚类中富集,称为 EMT 亚类,代谢途径、细胞-细胞连接和免疫反应在另一个亚类中占主导地位,称为代谢亚类。应用激酶活性预测算法并查询基因依赖性和药物敏感性数据库,预测雷帕霉素激酶(mTOR)和双特异性丝裂原活化蛋白激酶激酶 2(MAP2K2)分别是 EMT 和代谢亚型的潜在治疗靶点,这通过使用选择性抑制剂得到了证实。总体而言,我们的研究为胃癌蛋白质组学、激酶组学和分子分类学提供了新的、深入的见解,并揭示了潜在的治疗靶点,为精准治疗提供了基础。